{
  "id": 2937,
  "label": "multifocal dystonia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000478",
  "properties": {
    "xrefs": [
      "DOID:0050837",
      "GARD:0027527"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A dystonia that involves two or more unrelated body parts."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 5367,
      "label": "dystonic disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3996
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:543",
          "GARD:0027640",
          "HP:0001332",
          "ICD10CM:G24",
          "ICD9:333.90",
          "MEDGEN:3940",
          "MESH:D020821",
          "NCIT:C34563",
          "SCTID:15802004",
          "UMLS:C0013421"
        ],
        "synonyms": [
          "dystonia",
          "dystonic disorder",
          "dystonia disorder",
          "dystonia disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A movement disorder characterized by sustained or intermittent muscle contractions, resulting in abnormal movements and/or postures."
      },
      "child_count": 8,
      "reference_id": "MONDO:0003441"
    }
  ],
  "children": [
    {
      "id": 2945,
      "label": "hemidystonia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2937
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050846",
          "GARD:0027533",
          "ICD9:333.99",
          "MEDGEN:743329",
          "SCTID:427232004",
          "UMLS:C1960561"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A multifocal dystonia that involves the arm and leg on the same side of the body."
      },
      "child_count": 0,
      "reference_id": "MONDO:0000487"
    },
    {
      "id": 13829,
      "label": "dystonia 16",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2937,
        19719,
        20335
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090048",
          "GARD:0010539",
          "MEDGEN:436979",
          "MESH:C567430",
          "NANDO:1200529",
          "NCIT:C168729",
          "OMIM:612067",
          "Orphanet:210571",
          "SCTID:722435003",
          "UMLS:C2677567",
          "icd11.foundation:548945828"
        ],
        "synonyms": [
          "DYT-PRKRA",
          "DYT16",
          "PRKRA dystonic disorder",
          "dystonia 16",
          "dystonia type 16",
          "dystonic disorder caused by mutation in PRKRA",
          "early-onset dystonia parkinsonism",
          "Young-onset dystonia-(parkinsonism)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Dystonia 16 (DYT16) is a very rare and newly discovered movement disorder which is characterized by early-onset progressive limb dystonia, laryngeal and oromandibular dystonia, and parkinsonism."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012789"
    },
    {
      "id": 15043,
      "label": "dystonia 25",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2937,
        16634
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090055",
          "GARD:0010667",
          "MEDGEN:930339",
          "OMIM:615073",
          "Orphanet:329466",
          "UMLS:C4304670"
        ],
        "synonyms": [
          "GNAL dystonic disorder",
          "dystonia 25",
          "dystonia type 25",
          "dystonic disorder caused by mutation in GNAL",
          "DYT25",
          "autosomal dominant focal dystonia, DYT25 type"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal dominant focal dystonia, DTY25 is a form of focal dystonia, characterized by cervical, laryngeal and hand-forearm dystonia."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014033"
    }
  ],
  "roots": [
    {
      "id": 5367,
      "label": "dystonic disorder"
    }
  ]
}